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在原位大鼠模型中,硝普钠而非心房钠尿肽可抑制静脉收缩。

Nitroprusside, but not ANF inhibits venoconstriction in an in situ rat model.

作者信息

Watkins R W, Sybertz E J, Tedesco R P

机构信息

Department of Pharmacology, Schering Research, Bloomfield, NJ 07003.

出版信息

Eur J Pharmacol. 1987 Nov 17;143(3):299-304. doi: 10.1016/0014-2999(87)90453-5.

Abstract

Potential venodilator actions of nitroprusside (10 and 50 micrograms/min) and ANF (23 amino acid rat sequence, 10 and 30 micrograms/min) were assessed in rats subjected to cardiopulmonary bypass. Norepinephrine (NE, 10 micrograms) caused arterial pressor, i.e. increased perfusion pressure and venoconstrictor, i.e. increased venous flow, effects. ANF infusion failed to alter NE-induced pressor and venoconstrictor effects while nitroprusside significantly inhibited NE responses. Thus nitroprusside but not ANF, shows venodilator properties in this in situ rat model.

摘要

在接受体外循环的大鼠中评估了硝普钠(10和50微克/分钟)和心房钠尿肽(23个氨基酸的大鼠序列,10和30微克/分钟)的潜在血管舒张作用。去甲肾上腺素(NE,10微克)引起动脉升压作用,即灌注压升高,以及静脉收缩作用,即静脉血流增加。心房钠尿肽输注未能改变NE诱导的升压和静脉收缩作用,而硝普钠显著抑制NE反应。因此,在这个原位大鼠模型中,硝普钠而非心房钠尿肽表现出血管舒张特性。

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